CA2279131C - Separation electrophoretique des acides nucleiques des proteines a faible ph - Google Patents
Separation electrophoretique des acides nucleiques des proteines a faible ph Download PDFInfo
- Publication number
- CA2279131C CA2279131C CA2279131A CA2279131A CA2279131C CA 2279131 C CA2279131 C CA 2279131C CA 2279131 A CA2279131 A CA 2279131A CA 2279131 A CA2279131 A CA 2279131A CA 2279131 C CA2279131 C CA 2279131C
- Authority
- CA
- Canada
- Prior art keywords
- nucleic acids
- proteins
- electrophoresis
- rna
- protein
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 102000004169 proteins and genes Human genes 0.000 title claims abstract description 37
- 108090000623 proteins and genes Proteins 0.000 title claims abstract description 34
- 108020004707 nucleic acids Proteins 0.000 title abstract description 50
- 102000039446 nucleic acids Human genes 0.000 title abstract description 50
- 150000007523 nucleic acids Chemical class 0.000 title abstract description 50
- 238000000926 separation method Methods 0.000 title abstract description 12
- 238000001962 electrophoresis Methods 0.000 claims abstract description 33
- 238000000034 method Methods 0.000 claims abstract description 28
- 239000002253 acid Substances 0.000 claims abstract description 14
- 239000012472 biological sample Substances 0.000 claims abstract description 11
- 239000000523 sample Substances 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims description 8
- 210000002381 plasma Anatomy 0.000 claims description 5
- 230000005684 electric field Effects 0.000 claims description 4
- 238000000746 purification Methods 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract description 5
- 230000001413 cellular effect Effects 0.000 abstract description 4
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 16
- 239000000499 gel Substances 0.000 description 13
- 239000012528 membrane Substances 0.000 description 13
- 239000011543 agarose gel Substances 0.000 description 10
- 229920000936 Agarose Polymers 0.000 description 9
- 108020004414 DNA Proteins 0.000 description 9
- 108091005461 Nucleic proteins Proteins 0.000 description 8
- 238000003752 polymerase chain reaction Methods 0.000 description 8
- 241000700605 Viruses Species 0.000 description 5
- 239000000872 buffer Substances 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 230000003321 amplification Effects 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000003199 nucleic acid amplification method Methods 0.000 description 4
- 108020005075 5S Ribosomal RNA Proteins 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- 101710163270 Nuclease Proteins 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 244000309466 calf Species 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000000383 hazardous chemical Substances 0.000 description 3
- 238000001155 isoelectric focusing Methods 0.000 description 3
- 229920002521 macromolecule Polymers 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000002773 nucleotide Substances 0.000 description 3
- 125000003729 nucleotide group Chemical group 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000204031 Mycoplasma Species 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 2
- 102000006382 Ribonucleases Human genes 0.000 description 2
- 108010083644 Ribonucleases Proteins 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 230000003196 chaotropic effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- YMAWOPBAYDPSLA-UHFFFAOYSA-N glycylglycine Chemical compound [NH3+]CC(=O)NCC([O-])=O YMAWOPBAYDPSLA-UHFFFAOYSA-N 0.000 description 2
- 208000006454 hepatitis Diseases 0.000 description 2
- 231100000283 hepatitis Toxicity 0.000 description 2
- 238000001821 nucleic acid purification Methods 0.000 description 2
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- -1 pthalate Chemical compound 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 241001430294 unidentified retrovirus Species 0.000 description 2
- 108020004465 16S ribosomal RNA Proteins 0.000 description 1
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 description 1
- 101800000263 Acidic protein Proteins 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 238000000035 BCA protein assay Methods 0.000 description 1
- 102000004506 Blood Proteins Human genes 0.000 description 1
- 108010017384 Blood Proteins Proteins 0.000 description 1
- 241000589968 Borrelia Species 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 241000589876 Campylobacter Species 0.000 description 1
- 241000606161 Chlamydia Species 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 241000193163 Clostridioides difficile Species 0.000 description 1
- 201000003883 Cystic fibrosis Diseases 0.000 description 1
- 102000016928 DNA-directed DNA polymerase Human genes 0.000 description 1
- 108010014303 DNA-directed DNA polymerase Proteins 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 108010008488 Glycylglycine Proteins 0.000 description 1
- 241000606768 Haemophilus influenzae Species 0.000 description 1
- 206010020460 Human T-cell lymphotropic virus type I infection Diseases 0.000 description 1
- 241000714260 Human T-lymphotropic virus 1 Species 0.000 description 1
- 241000714259 Human T-lymphotropic virus 2 Species 0.000 description 1
- 241000701044 Human gammaherpesvirus 4 Species 0.000 description 1
- 208000026350 Inborn Genetic disease Diseases 0.000 description 1
- 241000589242 Legionella pneumophila Species 0.000 description 1
- 241000186781 Listeria Species 0.000 description 1
- 208000016604 Lyme disease Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241001502334 Mycobacterium avium complex bacterium Species 0.000 description 1
- 241000187479 Mycobacterium tuberculosis Species 0.000 description 1
- 241000202934 Mycoplasma pneumoniae Species 0.000 description 1
- 241000588653 Neisseria Species 0.000 description 1
- 101100457407 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) mmm-1 gene Proteins 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000233872 Pneumocystis carinii Species 0.000 description 1
- 241000725643 Respiratory syncytial virus Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000607142 Salmonella Species 0.000 description 1
- 241000607768 Shigella Species 0.000 description 1
- 241000700584 Simplexvirus Species 0.000 description 1
- 241000194017 Streptococcus Species 0.000 description 1
- 208000002903 Thalassemia Diseases 0.000 description 1
- 241000607734 Yersinia <bacteria> Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000007073 chemical hydrolysis Effects 0.000 description 1
- 229940001468 citrate Drugs 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 239000005549 deoxyribonucleoside Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 229940079920 digestives acid preparations Drugs 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000011842 forensic investigation Methods 0.000 description 1
- 229940050411 fumarate Drugs 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 208000016361 genetic disease Diseases 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 229940043257 glycylglycine Drugs 0.000 description 1
- 229940047650 haemophilus influenzae Drugs 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229940115932 legionella pneumophila Drugs 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 238000007834 ligase chain reaction Methods 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000012985 polymerization agent Substances 0.000 description 1
- 108091033319 polynucleotide Proteins 0.000 description 1
- 102000040430 polynucleotide Human genes 0.000 description 1
- 239000002157 polynucleotide Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000007065 protein hydrolysis Effects 0.000 description 1
- 244000000040 protozoan parasite Species 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 208000007056 sickle cell anemia Diseases 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 210000001541 thymus gland Anatomy 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- 125000002264 triphosphate group Chemical class [H]OP(=O)(O[H])OP(=O)(O[H])OP(=O)(O[H])O* 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1003—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Plant Pathology (AREA)
- Biophysics (AREA)
- Microbiology (AREA)
- Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Saccharide Compounds (AREA)
- Electrostatic Separation (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9525898P | 1998-08-04 | 1998-08-04 | |
| US60/095,258 | 1998-08-04 | ||
| US09/349,387 US6699986B2 (en) | 1998-08-04 | 1999-07-09 | Electrophoretic separation of nucleic acids from proteins at low ph |
| US09/349,387 | 1999-09-09 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2279131A1 CA2279131A1 (fr) | 2000-02-04 |
| CA2279131C true CA2279131C (fr) | 2010-12-14 |
Family
ID=26790014
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2279131A Expired - Fee Related CA2279131C (fr) | 1998-08-04 | 1999-07-29 | Separation electrophoretique des acides nucleiques des proteines a faible ph |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6699986B2 (fr) |
| EP (1) | EP0979868B1 (fr) |
| JP (1) | JP4531888B2 (fr) |
| AT (1) | ATE449843T1 (fr) |
| CA (1) | CA2279131C (fr) |
| DE (1) | DE69941655D1 (fr) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003302418A1 (en) * | 2002-11-28 | 2004-06-18 | Arkray Inc. | Method and apparatus for concentration and purification of nucleic acid |
| CN100491391C (zh) * | 2002-11-28 | 2009-05-27 | 爱科来株式会社 | 浓缩和纯化核酸的方法和装置 |
| JP2005110503A (ja) * | 2003-10-02 | 2005-04-28 | Arkray Inc | 核酸の精製方法及びデバイス |
| US20080035482A1 (en) * | 2003-11-10 | 2008-02-14 | Arkray Inc. | Method Of Concentrating And Purifying Nucleic Acid And Apparatus Therefor |
| KR100647306B1 (ko) * | 2004-12-23 | 2006-11-23 | 삼성전자주식회사 | 아미노기와 카르복실기를 포함하고 제1 pH에서 양전하를띠는 물질을 이용하여 핵산을 분리하는 방법 |
| US20080085563A1 (en) * | 2006-10-10 | 2008-04-10 | Idexx Laboratories, Inc. | Detection of Gadolinium Chelates |
| US20080085562A1 (en) * | 2006-10-10 | 2008-04-10 | Idexx Laboratories, Inc. | Detection of gadolinium chelates |
| US20140027282A1 (en) * | 2011-04-22 | 2014-01-30 | Sony Corporation | Method of electrophoresing nucleic acids, method of concentrating and purifying nucleic acids, cartridge for nucleic acid electrophoresis, and method of producing cartridge for nucleic acid electrophoresis |
| EP2773221B1 (fr) * | 2011-11-04 | 2019-01-09 | Bio-Rad Laboratories, Inc. | Purification simultanée de composants cellulaires |
| US9766207B2 (en) | 2011-11-04 | 2017-09-19 | Bio-Rad Laboratories, Inc. | Affinity methods and compositions employing electronic control of pH |
| EP2814597A4 (fr) | 2012-02-15 | 2015-10-28 | Bio Rad Laboratories | Régulation électronique de ph et de force ionique |
| US9321012B2 (en) | 2012-04-04 | 2016-04-26 | Bio-Rad Laboratories, Inc. | Electronic protein fractionation |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4750982A (en) | 1985-03-21 | 1988-06-14 | Lifecodes Corp. | Process and apparatus for purifying and concentrating DNA from crude mixtures containing DNA |
| US4965188A (en) | 1986-08-22 | 1990-10-23 | Cetus Corporation | Process for amplifying, detecting, and/or cloning nucleic acid sequences using a thermostable enzyme |
| US4683195A (en) | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US4822470A (en) * | 1987-10-09 | 1989-04-18 | Baylor College Of Medicine | Method of and apparatus for cell poration and cell fusion using radiofrequency electrical pulses |
| IE883226L (en) | 1988-10-25 | 1990-04-25 | Dna Prep Galway Ltd S 22 | Separation of nucleic acids from protein material using¹cation exchangers |
| US5386024A (en) | 1993-02-10 | 1995-01-31 | Gen-Probe Incorporated | Method to prepare nucleic acids from a biological sample using low pH and acid protease |
| US5635045A (en) * | 1993-05-20 | 1997-06-03 | Alam; Aftab | Apparatus for, and a method of, electroelution isolation of biomolecules and recovering biomolecules after elution |
| US5434270A (en) | 1994-09-15 | 1995-07-18 | Eastman Kodak Company | Weakly basic polymerizable monomers and polymers prepared therefrom |
| US5582988A (en) | 1994-09-15 | 1996-12-10 | Johnson & Johnson Clinical Diagnostics, Inc. | Methods for capture and selective release of nucleic acids using weakly basic polymer and amplification of same |
| US5973137A (en) | 1996-02-13 | 1999-10-26 | Gentra Systems, Inc. | Low pH RNA isolation reagents, method, and kit |
| DE19700364A1 (de) * | 1997-01-08 | 1998-07-09 | Bayer Ag | Elektrokinetische Probenvorbereitung |
-
1999
- 1999-07-09 US US09/349,387 patent/US6699986B2/en not_active Expired - Fee Related
- 1999-07-29 CA CA2279131A patent/CA2279131C/fr not_active Expired - Fee Related
- 1999-08-03 AT AT99306146T patent/ATE449843T1/de not_active IP Right Cessation
- 1999-08-03 EP EP99306146A patent/EP0979868B1/fr not_active Expired - Lifetime
- 1999-08-03 DE DE69941655T patent/DE69941655D1/de not_active Expired - Lifetime
- 1999-08-04 JP JP25207299A patent/JP4531888B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0979868A3 (fr) | 2001-07-18 |
| CA2279131A1 (fr) | 2000-02-04 |
| EP0979868A2 (fr) | 2000-02-16 |
| JP2000146911A (ja) | 2000-05-26 |
| ATE449843T1 (de) | 2009-12-15 |
| EP0979868B1 (fr) | 2009-11-25 |
| JP4531888B2 (ja) | 2010-08-25 |
| US20010049437A1 (en) | 2001-12-06 |
| DE69941655D1 (de) | 2010-01-07 |
| US6699986B2 (en) | 2004-03-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6914137B2 (en) | Isolation of nucleic acids | |
| CN1187362C (zh) | 核酸的固相分离法 | |
| EP0747388B1 (fr) | Méthode et équipement pour la purification d'acides nucléiques | |
| CA2279131C (fr) | Separation electrophoretique des acides nucleiques des proteines a faible ph | |
| US20150166592A1 (en) | Selective Nucleic Acid Fragment Recovery | |
| EP0969090A1 (fr) | Procédé rapide et simple pour l'isolation d'acide nucleique circulaire | |
| JPH09327291A (ja) | Rnaの抽出精製方法 | |
| JP3812696B2 (ja) | リボ核酸の抽出方法 | |
| US20230203476A1 (en) | Nucleic acid extraction method and application | |
| WO2001062976A1 (fr) | Methodes de separation, d'isolation et de purification rapides d'acide nucleique | |
| JPH1075784A (ja) | リボ核酸の単離方法 | |
| JPH11196869A (ja) | リボ核酸の単離方法 | |
| JP3922420B2 (ja) | 改良されたリボ核酸の単離方法 | |
| KR100624447B1 (ko) | 은 나노 입자를 이용한 핵산의 정제 방법 | |
| KR100563621B1 (ko) | 인간 혈액으로부터의 유전체 dna 추출용 키트 및이것을 이용한 유전체 dna 추출 방법 | |
| JP3811767B2 (ja) | 均質な混合物から核酸を純化する方法 | |
| HK1034520B (en) | Isolation of nucleic acids | |
| HK1034520A1 (en) | Isolation of nucleic acids |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20130730 |